Gene: TFRC ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11185506
rs11185506
TFRC
2 3 196070705 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs13072608
rs13072608
TFRC
2 3 196073396 intron variant C/T snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs2284889
rs2284889
TFRC
2 3 196061376 intron variant G/A snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs2284890
rs2284890
TFRC
2 3 196061276 intron variant T/C snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs2300774
rs2300774
TFRC
2 3 196066841 intron variant G/A snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs3326
rs3326
TFRC
2 3 196054635 intron variant G/A snv 0.30 0.700 1.000 1 2009 2009
dbSNP: rs3761717
rs3761717
TFRC
2 3 196071076 intron variant G/A;C snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs3804139
rs3804139
TFRC
2 3 196080754 intron variant T/C snv 0.49 0.700 1.000 1 2009 2009
dbSNP: rs9846149
rs9846149
TFRC
2 3 196060437 non coding transcript exon variant C/G snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs9858727
rs9858727
TFRC
2 3 196067370 intron variant A/T snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs9859401
rs9859401
TFRC
2 3 196073732 intron variant C/A;T snv 0.700 1.000 1 2009 2009